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Optimization of Coronary Heart Disease Chronic Disease Management Model Empowered by the 'Electrocardiogram Network' Platform under the Smart Hospital Framework and Effect Study: A Double-Center, Randomized, Single-Blind, Parallel-Controlled Clinical Trial

Optimization of Coronary Heart Disease Chronic Disease Management Model Empowered by the 'Electrocardiogram Network' Platform under the Smart Hospital Framework and Effect Study: A Double-Center, Randomized, Single-Blind, Parallel-Controlled Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120988
Enrollment
Unknown
Registered
2026-03-24
Start date
2026-03-26
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease

Interventions

Intervention Group :On the basis of conventional treatment, include the 'Electrocardiogram Network' platform for assisted management, implementing a digital chronic disease management model.
Control group:Standardized routine management based on current guidelines

Sponsors

People's Hospital of Jiang'an County
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years, no gender restriction; 2. Confirmed diagnosis of coronary heart disease (verified by coronary angiography, coronary CTA, previous PCI or CABG, or meeting relevant guideline diagnostic criteria); 3. In a stable phase, with no acute or unstable cardiovascular events in the past 4 weeks; 4. Presence of at least 2 cardiovascular metabolic risk factor abnormalities, with at least 1 being dyslipidemia (such as elevated LDL-C or currently receiving lipid-lowering treatment); 5. Able to understand the study content and complete follow-up; 6. Willing to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Presence of acute or unstable cardiovascular events within the past 4 weeks (such as acute myocardial infarction, unstable angina, acute heart failure, etc.); 2. Expected life expectancy <1 year; 3. Presence of severe mental, cognitive, or communication disorders that prevent completion of follow-up or relevant assessments; 4. Severe liver or kidney dysfunction, or other serious systemic diseases that may affect the judgment of study results; 5. Major interventions within the past 3 months that may significantly affect lipid, blood pressure, or glucose metabolism; 6. Currently participating in other clinical trials; 7. Other conditions deemed by the investigator as unsuitable for enrollment or difficult to complete follow-up.

Design outcomes

Primary

MeasureTime frame
Change in cardiometabolic composite score (?CCS) at 6 months;

Secondary

MeasureTime frame
LDL-C target achievement rate at 6 months (LDL-C <1.8 mmol/L);Major adverse cardiovascular events (cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, and urgent revascularization);Hospitalization and readmission (all-cause hospitalization, cardiovascular hospitalization, and readmission rates);Adherence measures (medication adherence, follow-up adherence, platform use adherence, and lifestyle adherence);Patient-reported outcomes (SAQ, PHQ-9, GAD-7, and PSQI scores);Angiographic outcomes in the PCI subgroup( late lumen loss );

Countries

China

Contacts

Public ContactChang Cheng

People's Hospital of Jiang'an County

937449609@qq.com+86 159 8310 3603

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 4, 2026